10 Panel CLIA Waived Drug Screen Dip Test – 25/Box (AMP / BAR / BZO / COC / mAMP / MTD / OPI / OXY / PCP / THC)

$78.75

CLIA Waived
FDA 510(k) Cleared
OTC & Rx Use

25 tests per box$3.15 per test

One-step urine drug screen dip test for the qualitative detection of 10 drugs and drug metabolites. Read results at 5 minutes.

  • Screens AMP, BAR, BZO, COC, mAMP/MET, MTD, OPI, OXY, PCP and THC
  • Single-use dip-card format for human urine
  • Up to 99% accurate
  • Up to 24-month shelf life
Quantity Discounts
1-5 6-10 11+
$78.75 $72.45 $68.51

10-Panel Drug Screen Dip Test Overview

The WDOA-4104 multi-drug urine test panel provides preliminary qualitative screening for amphetamine, barbiturates, benzodiazepines, cocaine metabolite, methamphetamine, methadone, opiates, oxycodone, phencyclidine and marijuana metabolite. Read results at 5 minutes and do not interpret results after 30 minutes. Each box contains 25 single-use test devices.

CLIA Waived
FDA 510(k) Cleared
OTC & Rx Use
25 Tests per Box

Features and Benefits

Ten-panel urine screeningOne device screens AMP, BAR, BZO, COC, mAMP/MET, MTD, OPI, OXY, PCP and THC.

Results at 5 minutesRead the drug-test results at 5 minutes and do not interpret them after 30 minutes.

Simple dip-card formatImmerse the absorbent end in a collected urine specimen and visually interpret the result lines.

Individually packagedEach box contains 25 single-use test devices in sealed pouches.

Up to 99% accuratePerformance varies by analyte and specimen concentration and depends on correct storage, testing and interpretation.

Up to 24-month shelf lifeAlways verify the expiration date printed on the sealed pouch or product packaging.

Product Details

Reference
WDOA-4104
SKU
DTK-209101
Sample
Human Urine
Package
25 Tests per Box

Specification Details
Test format One-step multi-panel urine dip card
Test method Competitive-binding lateral-flow immunochromatographic assay
Result type Preliminary qualitative screening result
Read time Read at 5 minutes; do not interpret after 30 minutes
Intended use Over-the-counter and prescription use
Regulatory status CLIA waived; FDA 510(k) cleared under K133968

Drug Panel and Cutoff Levels

This WDOA-4104 configuration screens for the following drugs and drug metabolites at the listed cutoff concentrations in human urine.

Detectable Drug or Drug Class Abbreviation Cutoff
Amphetamine AMP 1,000 ng/mL
Barbiturates BAR 300 ng/mL
Benzodiazepines BZO 300 ng/mL
Cocaine metabolite COC 300 ng/mL
Methamphetamine mAMP/MET 1,000 ng/mL
Methadone MTD 300 ng/mL
Opiates OPI 2,000 ng/mL
Oxycodone OXY 100 ng/mL
Phencyclidine PCP 25 ng/mL
Marijuana metabolite THC 50 ng/mL

Drug-detection periods vary with the substance, cutoff, dose, frequency and timing of use, specimen collection, individual metabolism and other biological factors. A screening result does not determine impairment. Follow the package insert supplied with the current lot when performing and interpreting the test.

How to Perform the Test

Prepare the testAllow the test and urine specimen to reach the temperature specified in the package insert. Open the sealed pouch and remove the device.

Expose the absorbent endHold the device by one side and remove the cap without touching the absorbent end.

Dip for approximately 10 secondsImmerse the absorbent end in the urine specimen without allowing the urine level to pass the marked maximum line.

Recap and readReplace the cap, lay the device flat on a clean, dry, non-absorbent surface and read the drug-test results at 5 minutes. Do not interpret results after 30 minutes.

Understanding the Results

NegativeA control line and the corresponding test line are visible. Any visible test line is interpreted as negative, regardless of its color intensity or width.

Preliminary positiveThe control line is visible, but no line appears in the corresponding test region. Confirm the result with a more specific analytical method.

InvalidNo control line appears. Repeat the test with a new device and follow the package insert.

Screening notice: This device provides only a preliminary qualitative result. A preliminary positive result should be confirmed using a more specific analytical method such as GC/MS or LC/MS-MS. Clinical consideration and professional judgment should be applied to any drug-test result.

Storage

Store the test in its sealed pouch at 39–86°F (4–30°C), protected from direct sunlight, moisture and heat. Do not freeze, and do not use the test after the expiration date printed on the packaging.

Instructions and Regulatory Documents

Frequently Asked Questions

What does the 10-panel dip test screen for?

WDOA-4104 screens urine for amphetamine, barbiturates, benzodiazepines, cocaine metabolite, methamphetamine, methadone, opiates, oxycodone, phencyclidine and marijuana metabolite at the cutoff concentrations shown above.

Does this configuration include MDMA or Ecstasy?

No. The exact WDOA-4104 configuration includes OXY rather than MDMA. The FDA device record lists AMP, BAR, BZO, COC, mAMP, MTD, OPI, OXY, PCP and THC.

Is WDOA-4104 CLIA waived?

Yes. The current Wondfo T-Dip product guide identifies WDOA-4104 as a CLIA-waived configuration.

Is this test intended for over-the-counter use?

Yes. FDA AccessGUDID lists the exact WDOA-4104 model for both over-the-counter and prescription use.

How quickly are results available?

Read the drug-test results at 5 minutes. Do not interpret the results after 30 minutes.

What specimen is required?

This dip test is designed for use with a collected human urine specimen.

What does a faint test line mean?

When the control line is present, any visible line in a test region is interpreted as negative, regardless of the test line’s color intensity or width.

Does a preliminary positive result require confirmation?

Yes. A preliminary positive screening result should be confirmed using a more specific analytical method such as GC/MS or LC/MS-MS.

How should the test be stored?

Store the sealed pouch at 39–86°F (4–30°C), protected from direct sunlight, moisture and heat. Do not freeze, and do not use a test beyond the expiration date printed on its packaging.

How many tests are included?

Each box contains 25 single-use test devices.

What are the accuracy and shelf-life claims?

DrugTestKitUSA currently lists this product as up to 99% accurate with an up to 24-month shelf life. Performance varies by analyte and specimen concentration and depends on correct storage, testing and interpretation. Always verify the expiration date on the individual product packaging.

Additional information

Weight 1 lbs
Dimensions 6 × 5 × 3 in

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